|Cosmo Artificial Intelligence Ltd./Cosmo Pharmaceuticals NV, of Dublin, and Medtronic plc, of Dublin||GI Genius||Computer-aided detection endoscopy module that uses artificial intelligence||Assists clinicians in detecting lesions in the colon in real time during a colonoscopy||U.S. FDA granted de novo clearance|
|Lucira Health Inc., of Emeryville, Calif.||Lucira Check It||At-home molecular test; available over the counter||For the qualitative detection of SARS-CoV-2||U.S. FDA issued emergency use authorization|
|Masimo Corp., of Irvine, Calif.||Radius PCG||Portable, real-time capnograph with Bluetooth connectivity; connects with the Root patient monitoring and connectivity platform||Measures, displays and monitors carbon dioxide partial pressure and respiratory rate during anesthesia, recovery and respiratory care||Received 510(k) clearance from the U.S. FDA|
|Myhomedoc Ltd., of Rahanana, Israel||Myhomedoc system||Hand-held multisensor device that pairs with a smartphone||For the remote examination of the mouth, throat, lungs, ears, heart, skin, abdomen, body temperature and oxygen saturation||Received 510(k) clearance from the U.S. FDA|
|Thermo Fisher Scientific Inc., of Waltham, Mass.||Applied Biosystems Taqpath COVID-19 Combo Kit||Real-time RT-PCR test||For the qualitative detection of nucleic acid from SARS-CoV-2 in upper respiratory specimens||U.S. FDA expanded emergency use authorization to include the Thermo Fisher Scientific Amplitude platform|
For more information about individual companies and/or products, see Cortellis.